10038-40-1

Usage

Uses

Used in Epoxy Resin Production:
2,2'-Bis(hydroxymethyl)diphenyl ether is used as a crosslinking agent for enhancing the structural integrity and performance of epoxy resins. This application is crucial in various industries due to the high demand for strong, durable, and heat-resistant materials.
Used in Adhesives Manufacturing:
In the adhesives industry, 2,2'-Bis(hydroxymethyl)diphenyl ether is used as a critical component to improve the bonding strength and flexibility of adhesives, making them suitable for a wide range of applications, from construction to automotive manufacturing.
Used in Protective Coatings:
2,2'-Bis(hydroxymethyl)diphenyl ether is utilized as a key ingredient in protective coatings to provide resistance against corrosion, wear, and environmental factors. Its inclusion in these coatings ensures the longevity and protection of various surfaces in industries such as aerospace, marine, and construction.
Used in Dental Sealants:
In the dental industry, 2,2'-Bis(hydroxymethyl)diphenyl ether is used as a component in dental sealants to protect teeth from decay and promote oral health. Its properties contribute to the sealants' durability and effectiveness in preventing dental caries.
Used in Pharmaceutical Synthesis:
As a precursor in the synthesis of certain pharmaceuticals, 2,2'-Bis(hydroxymethyl)diphenyl ether plays a significant role in the development of new drugs, highlighting its importance in the healthcare sector.
Despite these applications, the use of 2,2'-Bis(hydroxymethyl)diphenyl ether has faced scrutiny due to concerns over its potential health and environmental impacts, resulting in regulatory measures to limit its application in specific consumer products.

Upstream product

• 50-00-0 formaldehyd 
• 101-84-8 diphenylether 
• 446-52-6 2-Fluorobenzaldehyde 
• 90-02-8 salicylaldehyde 
• 49590-51-4 2,2'-oxybis(benzaldehyde) 
• 37424-29-6 2,2'-oxybis(benzoic acid) 
• 31680-22-5 2,2'-Oxybisbenzoesaeure-dimethylester 
• 32852-70-3 2,2'-oxy-di-benzoyl chloride 

Downstream Products

• 49590-51-4 2,2'-oxybis(benzaldehyde) 
• 18993-57-2 2,2'-oxybisbenzeneacetic acid 
• 132103-21-0 2,2'-oxybisbenzeneacetonitrile 
• 1356966-99-8 O(C₆H₄CH₂SH)2 
• 10038-41-2 2,2'-bis(bromomethyl)-1,1'-oxybisbenzene 

Relevant academic research and scientific papers

Gold(I) Complexes Stabilized by Nine- and Ten-Membered N-Heterocyclic Carbene Ligands

Nine- and ten-membered N-heterocyclic carbene (NHC) ligands have been developed and for the first time their gold(I) complexes were synthesized. The protonated NHC pro-ligands 2 a–h were prepared by the reaction of readily available N,N′-diarylformamidines with bis-electrophilic building blocks, followed by anion exchange. In situ deprotonation of the tetrafluoroborates 2 a–h with tBuOK in the presence of AuCl(SMe2) provided fast access to NHC-gold(I) complexes 3–10. These new NHC-gold(I) complexes show very good catalytic activity in a cycloisomerization reaction (0.1 mol % catalyst loading, up to 100 % conversion) and their solid-state structures reveal high steric hindrance around the metal atom (%Vbur up to 53.0) which is caused by their expanded-ring architecture.

Study on the intramolecular transannular chalcogen-tin interactions in dithiastannecine compounds

Dithiastannecine compounds of the type [{D(C6H 4CH2S)2}SnR1R2] with different donor atoms D were prepared, where D = O and R1 = R 2 = Ph (4a); R1 = Ph, Rsu

Potential Antitumor Agents. 62. Structure Activity Relationships for Tricyclic Compounds Related to the Colon Tumor Active Drug 9-Oxo-9H-xanthene-4-acetic Acid

A series of tricyclic analogues of 9-oxo-9H-xanthene-4-acetic acid have been prepared and evaluated for their ability to cause homorrhagic necrosis in subcutaneously implanted colon 38 tumors in mice, in an effort to extend the structure-activity relation